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AR070487A1 - DERIVATIVES OF 3- METHYL-IMIDAZO - (1,2-B) - PIRIDAZINA - Google Patents

DERIVATIVES OF 3- METHYL-IMIDAZO - (1,2-B) - PIRIDAZINA

Info

Publication number
AR070487A1
AR070487A1 ARP090100659A ARP090100659A AR070487A1 AR 070487 A1 AR070487 A1 AR 070487A1 AR P090100659 A ARP090100659 A AR P090100659A AR P090100659 A ARP090100659 A AR P090100659A AR 070487 A1 AR070487 A1 AR 070487A1
Authority
AR
Argentina
Prior art keywords
unsubstituted
formula
substituted
compound
halogen
Prior art date
Application number
ARP090100659A
Other languages
Spanish (es)
Original Assignee
Novartis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39672115&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR070487(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR070487A1 publication Critical patent/AR070487A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Un proceso para el tratamiento del cuerpo humano o animal, en particular con respecto una enfermedad mediada por la cinasa de tirosina c-Met; al uso de un compuesto de la formula (1) para la fabricacion de un medicamento para el tratamiento de estas enfermedades; a composiciones farmacéuticas que comprenden un compuesto de la formula (1), opcionalmente en la presencia de un componente de combinacion; y a procesos para la preparacion de un compuesto de la formula (1). Reivindicacion 1: Un compuesto de la formula (1) en donde: R1 representa heterociclilo insustituido o sustituido, arilo insustituido o sustituido, cicloalquilo insustituido o sustituido, alquilo insustituido o sustituido, alcoxilo insustituido o sustituido, ciano, carboxamida, o halogeno; R2 representa heterociclilo insustituido o sustituido, arilo insustituido o sustituido; R3 representa H, deuterio, alquilo inferior, y R3' representa H, deuterio, alquilo inferior, halogeno, hidroxilo, o R3 representa halogeno, y R3' representa halogeno, o R3 y R3' representan, junto con el átomo de carbono con el que están unidos, cicloalquilo o vinilo; A1 representa ya sea un enlace directo, un grupo -SO2-, o bien un grupo de formula (2) en donde el enlace marcado * está unido a R1; n representa 0 o 1; m representa 0, 1, 2, 3, 4 o 5; R4 representa H o alquilo insustituido; R5 representa H o alquilo insustituido; R5' representa H o alquilo insustituido; A2 representa O o NR4; o una sal del mismo.A process for the treatment of the human or animal body, in particular with respect to a disease mediated by tyrosine kinase c-Met; to the use of a compound of the formula (1) for the manufacture of a medicament for the treatment of these diseases; to pharmaceutical compositions comprising a compound of the formula (1), optionally in the presence of a combination component; and to processes for the preparation of a compound of the formula (1). Claim 1: A compound of the formula (1) wherein: R 1 represents unsubstituted or substituted heterocyclyl, unsubstituted or substituted aryl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted alkyl, unsubstituted or substituted alkoxy, cyano, carboxamide, or halogen; R2 represents unsubstituted or substituted heterocyclyl, unsubstituted or substituted aryl; R3 represents H, deuterium, lower alkyl, and R3 'represents H, deuterium, lower alkyl, halogen, hydroxyl, or R3 represents halogen, and R3' represents halogen, or R3 and R3 'represent, together with the carbon atom with the which are attached, cycloalkyl or vinyl; A1 represents either a direct link, a group -SO2-, or a group of formula (2) in which the labeled link * is attached to R1; n represents 0 or 1; m represents 0, 1, 2, 3, 4 or 5; R4 represents H or unsubstituted alkyl; R5 represents H or unsubstituted alkyl; R5 'represents H or unsubstituted alkyl; A2 represents O or NR4; or a salt thereof.

ARP090100659A 2008-02-28 2009-02-26 DERIVATIVES OF 3- METHYL-IMIDAZO - (1,2-B) - PIRIDAZINA AR070487A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08152068 2008-02-28

Publications (1)

Publication Number Publication Date
AR070487A1 true AR070487A1 (en) 2010-04-07

Family

ID=39672115

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP090100659A AR070487A1 (en) 2008-02-28 2009-02-26 DERIVATIVES OF 3- METHYL-IMIDAZO - (1,2-B) - PIRIDAZINA

Country Status (25)

Country Link
US (1) US8822468B2 (en)
EP (1) EP2265614A1 (en)
JP (1) JP5576802B2 (en)
KR (1) KR20100128305A (en)
CN (1) CN102015716B (en)
AR (1) AR070487A1 (en)
AU (1) AU2009218459A1 (en)
BR (1) BRPI0908504A2 (en)
CA (1) CA2717034A1 (en)
CL (1) CL2009000443A1 (en)
CO (1) CO6300957A2 (en)
CR (1) CR11620A (en)
DO (1) DOP2010000263A (en)
EA (1) EA201001365A1 (en)
EC (1) ECSP10010427A (en)
IL (1) IL207434A0 (en)
MA (1) MA32167B1 (en)
MX (1) MX2010009414A (en)
NI (1) NI201000145A (en)
PE (1) PE20091468A1 (en)
SM (1) SMAP201000112A (en)
TW (1) TW200940545A (en)
UY (1) UY31676A1 (en)
WO (1) WO2009106577A1 (en)
ZA (1) ZA201005602B (en)

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BR112012003262A8 (en) 2009-08-12 2016-05-17 Novartis Ag Heterocyclic Hydrazone Compounds and Their Uses to Treat Cancer and Inflammation
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US20110195066A1 (en) * 2010-02-05 2011-08-11 Auspex Pharmaceuticals, Inc. Quinoline inhibitors of tyrosine kinase
WO2012003338A1 (en) * 2010-07-01 2012-01-05 Takeda Pharmaceutical Company Limited COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET
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EP2755976B1 (en) 2011-09-15 2018-07-18 Novartis AG 6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyridines as c-met tyrosine kinase inhibitors
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WO2014138692A1 (en) 2013-03-07 2014-09-12 Califia Bio, Inc. Mixed lineage kinase inhibitors and method of treatments
AR097543A1 (en) * 2013-09-06 2016-03-23 Lexicon Pharmaceuticals Inc COMPOUNDS BASED ON IMIDAZO [1,2-b] PIRIDAZINE, COMPOSITIONS THAT INCLUDE THEM AND THEIR METHODS OF USE
CN105326793A (en) * 2014-08-06 2016-02-17 中美冠科生物技术(太仓)有限公司 Solid dispersion containing c-Met kinase inhibitor and preparation method and application of solid dispersion
CN107108633B (en) * 2014-12-19 2020-05-12 詹森药业有限公司 Heterocyclyl-linked imidazopyridazine derivatives as PI3K β inhibitors
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EP3512852B1 (en) * 2016-09-16 2024-06-26 Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) Traf 6 inhibitors
EP3558304A2 (en) * 2016-12-23 2019-10-30 Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) Inhibitors of cytochrome p450 family 7 subfamily b member 1 (cyp7b1) for use in treating diseases
WO2018138050A1 (en) 2017-01-26 2018-08-02 Bayer Aktiengesellschaft Condensed bicyclic heterocyclene derivatives as pest control agents
US11584744B2 (en) * 2017-06-23 2023-02-21 University Of Washington Inhibitors of type 1 methionyl-tRNA synthetase and methods of using them
JP7296992B2 (en) * 2018-05-28 2023-06-23 エフ. ホフマン-ラ ロシュ アーゲー Novel oxoquinolidine compounds for the treatment and prevention of bacterial infections
JP7712932B2 (en) * 2019-12-18 2025-07-24 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア LIN28 INHIBITORS AND METHODS OF USE THEREOF
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Also Published As

Publication number Publication date
JP5576802B2 (en) 2014-08-20
BRPI0908504A2 (en) 2015-08-11
US20090264406A1 (en) 2009-10-22
SMAP201000112A (en) 2010-11-12
MX2010009414A (en) 2010-09-24
AU2009218459A1 (en) 2009-09-03
TW200940545A (en) 2009-10-01
EA201001365A1 (en) 2011-04-29
UY31676A1 (en) 2009-09-30
ECSP10010427A (en) 2010-09-30
NI201000145A (en) 2011-03-02
CR11620A (en) 2010-10-08
IL207434A0 (en) 2010-12-30
ZA201005602B (en) 2011-04-28
WO2009106577A1 (en) 2009-09-03
EP2265614A1 (en) 2010-12-29
CO6300957A2 (en) 2011-07-21
JP2011513279A (en) 2011-04-28
CN102015716A (en) 2011-04-13
DOP2010000263A (en) 2010-09-30
CN102015716B (en) 2014-09-17
KR20100128305A (en) 2010-12-07
PE20091468A1 (en) 2009-10-22
MA32167B1 (en) 2011-03-01
US8822468B2 (en) 2014-09-02
CA2717034A1 (en) 2009-09-03
CL2009000443A1 (en) 2010-09-10

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